首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Intravenous Laser Blood Irradiation Increases Efficacy of Etanercept in Selected Subtypes of Juvenile Idiopathic Arthritis: An Innovative Clinical Research Approach
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Intravenous Laser Blood Irradiation Increases Efficacy of Etanercept in Selected Subtypes of Juvenile Idiopathic Arthritis: An Innovative Clinical Research Approach

机译:静脉内激光血液辐照提高青少年特发性关节炎某些亚型中依那西普的功效:一种创新的临床研究方法

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摘要

This single-blind, placebo-controlled study assesses the efficacy of synergic administration of intravenous laser blood irradiation (ILBI) and etanercept in selected subtypes of juvenile idiopathic arthritis (JIA). Etanercept is a tumor necrosis factor alpha blocking agent with recognized importance in JIA. Laser radiation has immunomodulatory effects in animal and human studies. Fourteen patients (Group I) received ILBI and 9 patients (Group II) received placebo laser. ILBI was performed in addition to ongoing JIA medication, including etanercept. ILBI was administrated in 3 sets of 5 consecutive daily sessions, with a 7-week interval between every set of sessions. Evaluation was performed using ACR (American College of Rheumatology) Pediatric Criteria (ACR Pedi) at study enrollment and at 10 and 20 weeks, respectively. After 10 weeks, 85.7% of the patients in Group I fulfilled Pedi 30 criteria, compared to only 55.6% of the patients in Group II. After 20 weeks, all patients in both groups had a Pedi 30 response. In Group I, 92.8% of the subjects met the Pedi 50 response, compared to only 55.6% in the placebo group. One patient in Group I responded best, fulfilling Pedi 70 criteria. If applied synergistically, ILBI and etanercept would have an increased efficacy in promoting JIA remission.
机译:这项单盲,安慰剂对照的研究评估了在青少年特发性关节炎(JIA)选定亚型中静脉内激光血放射(ILBI)和依那西普的协同给药效果。 Etanercept是一种肿瘤坏死因子α阻断剂,在JIA中具有重要意义。激光辐射在动物和人体研究中具有免疫调节作用。 14名患者(I组)接受了ILBI治疗,9名患者(II组)接受了安慰剂激光治疗。除正在进行的JIA药物(包括依那西普)外,还进行了ILBI治疗。 ILBI分为3组,每组5个连续的每日课程,每组之间间隔7周。在研究入组时和分别在10周和20周时,使用ACR(美国风湿病学会)儿科标准(ACR Pedi)进行评估。 10周后,I组患者中有85.7%满足Pedi 30标准,而II组患者中只有55.6%。 20周后,两组中的所有患者均出现Pedi 30反应。在第一组中,有92.8%的受试者达到了Pedi 50反应,而在安慰剂组中只有55.6%。第一组患者中,满足Pedi 70标准的患者反应最好。如果协同应用,ILBI和依那西普在促进JIA缓解方面将具有更高的功效。

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